Power generation method for solid alkaline fuel cell

ABSTRACT

A method of power generation for a solid alkaline fuel cell includes the step of exposing a cathode-side surface of the inorganic solid electrolyte to an atmosphere containing carbon dioxide of greater than or equal to 600 ppm and less than or equal to 20000 ppm.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation application of PCT/JP2018/046345, filed Dec. 17, 2018, which claims priority to Japanese Application No. 2017-241274, filed Dec. 18, 2017, the entire contents all of which are incorporated hereby by reference.

TECHNICAL FIELD

The present invention relates to a power generation method for a solid alkaline fuel cell.

BACKGROUND ART

Alkaline fuel cells (AFC) are known as a fuel cell that operates at a relatively low temperature (for example, less than or equal to 250 degrees C.). Various liquid fuels or gaseous fuels can be used in an AFC and for example, use of methanol as a fuel causes the following electrochemical reaction. Anode: CH₃OH+6OH⁻→6e⁻+CO₂+5H₂O Cathode: 3/2O₂+3H₂O+6e⁻→6OH⁻ Overall: CH₃OH+3/2O₂→CO₂+2H₂O

In this context, Japanese Patent Application Laid-Open No. 2016-071948 proposes a solid alkaline fuel cell in which an inorganic solid electrolyte that exhibits hydroxide ion conductivity is configured as a layered double hydroxide (LDH) that does not exhibit liquid permeability and gas permeability.

LDH is expressed by the general formula [M²⁺ _(1-x)M³⁺ _(x)(OH)₂] [A^(n−) _(x/n).mH₂O] (wherein M²⁺ is a divalent cation, M³⁺ is a trivalent cation, and A^(n−) is an n-valent anion).

LDH has a layered structure in which anions and water that correspond to the second half of the above general formula are retained between double hydroxide layers that correspond to the first half of the general formula. A double hydroxide layer is configured as a solid solution of trivalent metal ions in a divalent metal hydroxide and exhibits a positive charge. The anions between the layers exhibit a negative charge to thereby compensate for the positive charge of the double hydroxide layer.

SUMMARY OF INVENTION

It is desirable to enhance the power generation capacity of a solid alkaline fuel cell by improving the hydroxide ion conductivity of the LDH.

As a result of investigations performed by the present inventors, the new insight has been gained that it is possible to improve the stability of anions that are coordinated between the layers of LDH and as a result improve hydroxide ion conductivity by exposing the cathode-side surface of LDH to an atmosphere containing a predetermined concentration of carbon-dioxide.

The present invention is proposed based on the new insight above, and has the object of providing a method of power generation for a solid alkaline fuel cell that enhances the power generation capacity.

Solution to Problem

A method of power generation for a solid alkaline fuel cell according to the present invention is a method for a solid alkaline fuel cell having a cathode, an anode, and an inorganic solid electrolyte which is disposed between the anode and the cathode and which exhibits hydroxide ion conductivity, and includes the step of exposing a cathode-side surface of the inorganic solid electrolyte to an atmosphere containing carbon dioxide of greater than or equal to 600 ppm and less than or equal to 20000 ppm.

The present invention provides a method of power generation for a solid alkaline fuel cell that enhances the power generation capacity.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is a cross sectional view illustrating a schematic configuration of a solid alkaline fuel cell.

FIG. 2 is an exploded perspective view illustrating a solid alkaline fuel cell according to an Example.

DESCRIPTION OF EMBODIMENTS

Solid Alkaline Fuel Cell 10

A solid alkaline fuel cell 10 is a type of alkaline fuel cell (AFC) that operates at a relatively low temperature. The operation temperature of the solid alkaline fuel cell 10 according to the present embodiment is 50 degrees C. to 250 degrees C. The solid alkaline fuel cell 10 operates for example with methanol and generates power with the electrochemical reaction below. Cathode 12: 3/2O₂+3H₂O+6e⁻→6OH⁻ Anode 14: CH₃OH+6OH⁻→6e⁻+CO₂+5H₂O Overall: CH₃OH+3/2O₂→CO₂+2H₂O

FIG. 1 is a cross sectional view illustrating a schematic configuration of the solid alkaline fuel cell 10. The solid alkaline fuel cell 10 includes a cathode 12, an anode 14, and an inorganic solid electrolyte 16.

The cathode 12 is a positive electrode that is generally termed the air electrode. During power generation by the solid alkaline fuel cell 10, an oxidant supply means 13 supplies the cathode 12 with an oxidant that includes oxygen (O₂). The oxidant may include use of air. Furthermore, it is preferred that the oxidant contains water (H₂O) as required. The oxidant for example may include use of air and humidified air, or the like.

The term “water (H₂O)” as used in the specification may denote water vapor in a gaseous state, moisture in a liquid state, and a gas-liquid mixture of water vapor and moisture.

The cathode 12 may be configured to include a known cathode catalyst that is used in an alkaline fuel cell, but there is no limitation in this regard. An example of a cathode catalyst includes a group 8 to 10 element (an element that belongs to groups 8 to 10 in the IUPAC format periodic table) such as a platinum group element (Ru, Rh, Pd, Os, Ir, Pt), an iron group element (Fe, Co, Ni), or the like, a group 11 element (an element that belongs to group 11 in the IUPAC format periodic table) such as Cu, Ag, Au, or the like, rhodium phthalocyanine, tetraphenylporphyrin, Co salen, Ni salen (salen=N,N′-bis (salicylidene) ethylenediamine), silver nitrate, and arbitrary combinations thereof. Although there is no particular limitation in relation to the amount of supported catalyst in the cathode 12, a value of 0.1 to 10 mg/cm² is preferred, and 0.1 to 5 mg/cm² being more preferred. It is preferred that the cathode catalyst is supported on carbon. A preferred example of the cathode 12 or a catalyst that used to configure the cathode 12 includes platinum-supporting carbon (Pt/C), paladium-supporting carbon (Pd/C), rhodium-supporting carbon (Rh/C), nickel-supporting carbon (Ni/C), copper-supporting carbon (Cu/C) and silver-supporting carbon (Ag/C).

Although there is no particular limitation in relation to the method of preparation for the cathode 12, for example, it may be formed by mixing a cathode catalyst with a support and a binder as desired to form a paste, and coating the paste mixture onto one surface of the inorganic solid electrolyte 16.

The anode 14 is a negative electrode that is generally termed the fuel electrode. During power generation by the solid alkaline fuel cell 10, a fuel supply means 15 supplies the anode 14 with a fuel. The fuel may be configured as either a liquid fuel or gaseous fuel. A liquid fuel may be a liquid of a fuel compound itself, or may be a solid fuel compound that has been dissolved in a liquid such as water, alcohol, or the like.

For example, the fuel compound includes (i) types of hydrazine such as hydrazine (NH₂NH₂), hydrated hydrazine (NH₂NH₂.H₂O), hydrazine carbonate ((NH₂NH₂)₂CO₂), hydrazine sulfate (NH₂NH₂.H₂SO₄), monomethyl hydrazine (CH₃NHNH₂), dimethyl hydrazine ((CH₃)₂ NNH₂, CH₃NHNHCH₃) and carboxylic hydrazide ((NHNH₂)₂CO), or the like, (ii) urea (NH₂CONH₂), (iii) ammonia (NH₃), (iv) heterocyclic compounds such as imidazole, 1,3,5-triazine, 3-amino-1,2,4 -triazole, or the like, and (v) hydroxylamines such as hydroxylamine (NH₂OH), hydroxylamine sulfate (NH₂OH.H₂SO₄), or the like, and combinations thereof.

Those compounds of the above fuel compounds that do not contain carbon (that is to say, hydrazine, hydrated hydrazine, hydrazine sulfate, ammonia, hydroxylamine, hydroxylamine sulfate, or the like) not only enable enhanced durability by avoiding any problems associated with catalyst poisoning by carbon monoxide, but also avoid carbon dioxide emissions.

The fuel compound may be used without modification as a fuel or may be used as a solution by dissolving in water and/or alcohol (for example, a lower alcohol such as methanol, ethanol, propanol, isopropanol, or the like). For example, since fuel compounds such as hydrazine, hydrated hydrazine, monomethyl hydrazine and dimethyl hydrazine are in a liquid state, use is possible as a liquid fuel without modification. Furthermore, solids such as hydrazine carbonate, hydrazine sulfate, carboxylic hydrazide, urea, imidazole, 3-amino-1,2,4 -triazole and hydroxylamine sulfate can be dissolved in water. Solids such as 1,3,5-triazine and hydroxylamine can be dissolved in alcohol. A gas such as ammonia can be dissolved in water. In this manner, solid fuel compounds can be used as a liquid fuel by dissolution in water or alcohol. When using a fuel compound by dissolution in water and/or alcohol, the concentration of the fuel compound in solution for example is 1 to 90 wt % and is preferably 1 to 30 wt %.

Furthermore, hydrocarbon liquid fuels that include types of ethers or types of alcohol such as methanol, ethanol, or the like, hydrocarbon gases such as methane or the like, or pure hydrogen or the like may be used as a fuel without modification. In particular, methanol is suitable as a fuel for use in the solid alkaline fuel cell 10 according to the present embodiment. Methanol may be in gaseous state, liquid state or as a gas-liquid mixture.

Although the anode 14 may be configured to include a known anode catalyst that is used in an alkaline fuel cell, there is no particular limitation in this regard. An example of an anode catalyst includes a metal catalyst such as Pt, Ni, Co, Fe, Ru, Sn and Pd or the like. Although it is preferred that a metal catalyst is supported on a support such as carbon or the like, it may be configured as an organometal complex using the metal atoms of the metal catalyst as the central metal, or supported by use of such an organometal complex as a support. Furthermore, a diffusion layer that is configured using a porous material or the like may be disposed on a surface of the anode catalyst. Preferred examples of the anode 14 or the catalyst that is used to configure the anode include nickel, cobalt, silver, platinum supporting carbon (Pt/C), palladium supporting carbon (Pd/C), rhodium supporting carbon (Rh/C), nickel supporting carbon (Ni/C), copper supporting carbon (Cu/C) and silver supporting carbon (Ag/C).

Although there is no particular limitation in relation to the method of preparation for the anode 14, for example, it may be formed by mixing an anode catalyst with a support and a binder as desired to form a paste, and coating the paste mixture onto the surface of the inorganic solid electrolyte 16 that is opposite to the cathode 12.

The inorganic solid electrolyte 16 is disposed between the cathode 12 and the anode 14. The inorganic solid electrolyte 16 includes a cathode-side surface 16S and an anode-side surface 16T. The cathode-side surface 16S is a region in the outer surface of the inorganic solid electrolyte 16 that is exposed in a space in which the cathode 12 is disposed, and faces the cathode 12. The anode-side surface 16T is a region in the outer surface of the inorganic solid electrolyte 16 that is exposed in a space in which the anode 14 is disposed, and faces the anode 14.

The inorganic solid electrolyte 16 is configured as a layered double hydroxide (referred to below as “LDH”) that exhibits hydroxide ion conductivity. The inorganic solid electrolyte 16 exhibits superior heat resistance and durability when compared with a configuration in which an organic material such as AEM (anion exchange membrane) is used as an electrolyte. The higher the hydroxide ion conductivity in the inorganic solid electrolyte 16, the more such a configuration is preferred and it is typically configured as 10⁻⁴ to 10⁻¹ S/m.

LDH has a basic composition that is expressed by the general formula of [M²⁺ _(1-x)M³⁺ _(x)(OH)₂] [A^(n−) _(x/n).mH₂O] (wherein M²⁺ is a divalent cation, M³⁺ is a trivalent cation, and A^(n−) is an n-valent anion, n is an integer that is greater than or equal to 1, and x takes a value of 0.1 to 0.4).

LDH has a layered structure in which anions and water that correspond to the second half of the above general formula are retained between double hydroxide layers that correspond to the first half of the general formula. A double hydroxide layer is configured as a solid solution of trivalent metal ions in a divalent metal hydroxide and exhibits a positive charge. The anions between the layers exhibit a negative charge to thereby compensate for the positive charge of the double hydroxide layer

In the general formula above, although M²⁺ may be an arbitrary divalent cation, it preferably includes Mg²⁺, Ca²⁺, and Zn²⁺, and more preferably is Mg²⁺. M³⁺ may be an arbitrary trivalent cation, preferably includes Al³⁺ or Cr³⁺, and more preferably is Al³⁺. A^(n−) is an arbitrary anion, preferably includes OH⁻ and CO₃ ²⁻.

Therefore in the general formula above, it is particularly preferred that M²⁺ includes Mg²⁺, M³⁺ includes Al³⁺ and A^(n−) includes OH⁻ and CO₃ ²⁻. Although n is an integer that is greater than or equal to 1, it preferably takes a value of 1 or 2. Although x takes a value of 0.1 to 0.4, it preferably takes a value of 0.2 to 0.35. An arbitrary real number is denoted by m.

Furthermore, a portion or all of M³⁺ in the general formula above may be substituted by cations having a valency of 4 or more, and in that configuration, the coefficient x/n of the anion A^(n−) in the general formula may be suitably varied.

In this context, during power generation by the solid alkaline fuel cell 10, the cathode-side surface 16S of the inorganic solid electrolyte 16 according to the present embodiment is exposed to an atmosphere containing carbon dioxide of greater than or equal to 600 ppm and less than or equal to 20000 ppm. In this manner, it is possible to enhance the stability of anions that are coordinated between the LDH layers by operation (power generation) in a state in which the cathode-side surface 16S is exposed to an atmosphere containing the above concentration range of carbon-dioxide. As a result, power generation of the solid alkaline fuel cell 10 can be enhanced by improving the hydroxide ion conductivity of the inorganic solid electrolyte 16.

The following first method, second method, third method, or a combination of any of the first to the third methods may be adopted to thereby expose the cathode-side surface 16S to an atmosphere having the above concentration range of carbon-dioxide.

The first method is a method of including carbon dioxide in the oxidant that is supplied by the oxidant supply means 13 to the cathode 12. In this configuration, the oxidant will contain carbon dioxide within the above concentration range in addition to water and oxygen. When humidified air is used as the oxidant, a desired concentration of carbon dioxide may be added to the humidified air by taking into account the concentration of carbon dioxide that is contained in the air.

The second method is a method of providing through holes in the inorganic solid electrolyte 16. The through holes may be formed by piercing an inner portion of the inorganic solid electrolyte 16 from the anode-side surface 16T to the cathode-side surface 16S without any particular limitation in relation to their shape. The through holes enable permeation to the cathode 12 of fuel that is supplied to the anode 14 and carbon dioxide that is produced by the electrochemical reaction at the anode 14. Carbon dioxide is produced when oxygen that is contained in the oxidant reacts with the fuel that has permeated through the through holes to the cathode 12. For example, when methanol is used as a fuel, the following reaction occurs at the cathode 12. Cathode 12: CH₃OH+3/2O₂→CO₂+2H₂O

In this manner, the second method uses carbon dioxide that is produced from fuel that has permeated through the through holes to the cathode 12 and carbon dioxide that is produced by the electrochemical reaction at the anode 14. The inner diameter and number of the through holes may be suitably set to so that the carbon dioxide concentration in proximity to the cathode-side surface 16S of the inorganic solid electrolyte 16 falls within the above concentration range. When humidified air is used as an oxidant, the inner diameter and number of the through holes may be set by taking into account the concentration of carbon dioxide that is contained in air. The through holes are preferably disposed in proximity to the supply port of the oxidant supply means 13 in the inorganic solid electrolyte 16. In this manner, carbon dioxide that is produced by a reaction of between oxygen and the fuel that flows from the through holes to the cathode 12 can be transferred together with the oxidant to the whole cathode 12.

The third method is a method of providing pores in the inorganic solid electrolyte 16. It is preferred that the pores are formed to connect an inner portion of the inorganic solid electrolyte 16 from the anode-side surface 16T to the cathode-side surface 16S. The pores enable permeation to the cathode 12 of fuel that is supplied to the anode 14 and carbon dioxide that is produced by the electrochemical reaction at the anode 14. In the same manner as the second method as described above, the third method uses carbon dioxide that is produced from fuel that has permeated through the pores to the cathode 12 and carbon dioxide that is produced by the electrochemical reaction at the anode 14. There is no particular limitation on the shape of the pores, and they may be configured with an irregular shape, or as a mesh or the like. The pores may be formed throughout the inorganic solid electrolyte 16, or may be formed only in a portion of the inorganic solid electrolyte 16. The inner diameter, length and number of the pores may be suitably set to so that the carbon dioxide concentration in proximity to the cathode-side surface 16S of the inorganic solid electrolyte 16 falls within the above concentration range. When humidified air is used as an oxidant, the inner diameter and number of the pores may be set by taking into account the concentration of carbon dioxide that is contained in air.

It is noted that a configuration in which the cathode-side surface 16S of the inorganic solid electrolyte 16 is exposed to an atmosphere containing carbon dioxide within the above concentration range means that the cathode 14 is also necessarily exposed to an atmosphere containing carbon dioxide. However since carbon dioxide is an inert gas, there is almost no effect on the catalyst activity of the cathode 14.

Although the inorganic solid electrolyte 16 may be configured only by use of a particle group that contains LDH, an additive component to assist in the density or hardness of that particle group may also be included.

The inorganic solid electrolyte 16 may be configured as a complex using a substrate formed as a porous body that exhibits an open pore configuration and LDH that is precipitated and grown into the pores to thereby fill the pores of the porous body. The porous body may be configured by a ceramic material such as alumina, zirconia or the like or an insulating material such as a porous sheet or the like that is formed from a foam resin or fibrous substance.

The inorganic solid electrolyte 16 may be configured in any of a plate shape, membrane shape or stacked shape. When the inorganic solid electrolyte 16 has a membrane or stacked shape, the membrane or stacked shaped LDH of the inorganic solid electrolyte 16 may be formed in the porous substrate or on the porous substrate. When the inorganic solid electrolyte 16 has a membrane or stacked shape, the thickness of the inorganic solid electrolyte 16 may be configured as less than or equal to 100 μm, preferably less than or equal to 75 μm, more preferably less than or equal to 50 μm, still more preferably less than or equal to 25 μm, and particularly more preferably less than or equal to 5 μm. The resistance of the inorganic solid electrolyte 16 decreases as the thickness of the inorganic solid electrolyte 16 is reduced. The lower limiting value of the thickness of the inorganic solid electrolyte 16 may be set with reference to a given use, but is preferably greater than or equal to 1 μm and more preferably greater than or equal to 2 μm in order to maintain a certain degree of rigidity. When the inorganic solid electrolyte 16 has a plate shape, the thickness of the inorganic solid electrolyte 16 may be configured as 0.01 to 0.5 mm, preferably 0.02 to 0.2 mm, and more preferably 0.05 to 0.1 mm.

Method of Manufacturing Inorganic Solid Electrolyte 16

An example of a method of manufacturing an inorganic solid electrolyte 16 will be described. The method of manufacture in the following description is performed by molding and firing an LDH powder that is typically hydrotalcite to thereby form an oxide fired body, and then regenerating the fired body to LDH and removing excess moisture. The method of manufacture enables simple and stable manufacture of a dense inorganic solid electrolyte 16.

1. Preparation of LDH Powder

An LDH powder is prepared that has a basic composition expressed by the general formula above: [M²⁺ _(1-x)M³⁺ _(x)(OH)₂] [A^(n−) _(x/n).mH₂O] (wherein M²⁺ is a divalent cation, M³⁺ is a trivalent cation, and A^(n−) is an n-valent anion, n is an integer greater than or equal to 1, and x is 0.1 to 0.4). This type of LDH powder is commercially available, or is a starting material that is prepared by use of a known method such as a liquid phase synthesis method or the like that uses sulfate salts or chlorides.

Although there is no particular limitation on the particle diameter of the LDH powder, a volume reference D50 average particle diameter is preferably 0.1 μm to 1.0 μm, and more preferably 0.3 μm to 0.8 μm. When the particle diameter of the LDH powder is excessively fine, the powder aggregates and tends to cause residual pores during molding. An excessively large particle diameter of the LDH powder has an adverse effect on molding characteristics.

The LDH powder may be calcined into an oxide powder. The calcine temperature in that case may be set within a temperature range that does not greatly change the starting material particle diameter and, for example, is preferably less than or equal to 500 degrees C., and more preferably 380 degrees C. to 460 degrees C.

2. Preparation of Green Body

Next, the LDH powder is molded to form a green body. The molding step is preferably performed by pressure molding for example so that the relative density of the green body is 43% to 65%, more preferably 45% to 60%, and still more preferably 47% to 58%. The pressure molding may be performed by use of a known method such as a mold uniaxial press, cold isostatic pressurization (CIP), slip casting, or extrusion molding, or the like. However, when the LDH powder is calcined to form an oxide powder, there is a limitation to dry molding methods.

When the inorganic solid electrolyte 16 is exposed to an atmosphere containing carbon dioxide within the above concentration range by use of the third method (method of provision of pores) as described above, the green body is formed by addition of a pore forming agent (for example, an acrylate polymer, methylcellulose or the like) to the LDH powder. Pores are formed in an inner portion of the oxide fired body by firing and removal of the pore forming agent in a firing step as described below. The inner diameter, length and number of pores may be adjusted by the amount and the particle diameter of the pore forming agent.

The relative density of the green body is calculated by using a theoretical density to divide the density that is calculated with reference to the weight and dimensions of the green body. Since the weight of the green body is affected by adsorbed moisture, a unique value is preferably obtained by measuring a green body that is configured from LDH powder that has been stored for greater than or equal to 24 hours at room temperature in a desiccator in a relative humidity of less than or equal to 20%, or by measuring the relative density of the green body after storage under the above conditions.

However, when the LDH powder is calcined to form an oxide powder, the relative density of the green body is preferably 26% to 40% and more preferably 29% to 36%. The relative density when using an oxide powder assumes that the respective metal elements that configure the LDH are converted into their respective oxides by calcining, and is calculated using a denominator that is calculated as a converted density of a mixture of each oxide.

3. Firing Step

Next, the green body is fired to form an oxide fired body. The firing step is preferably performed so that the oxide fired body has a weight that is 57% to 65% of the weight of the green body, and/or a volume that is 70% to 76% of the volume of the green body.

A configuration in which the weight of the oxide fired body is greater than or equal to 57% of the weight of the green body inhibits the formation of heterogeneous phases that are not regenerated during regeneration to LDH in subsequent steps. A configuration in which it is less than or equal to 65% of the weight of the green body enables the formation of a sufficient density in the following steps in response to sufficient firing. Furthermore a configuration in which the volume of the oxide fired body is greater than or equal to 70% of the volume of the green body inhibits the formation of heterogeneous phases that are not regenerated during regeneration to LDH in subsequent steps, and inhibits the formation of cracks. A configuration when it is less than or equal to 76% the volume of the green body enables the formation of a sufficient density in the following steps in response to sufficient firing.

However, when the LDH powder is calcined to form an oxide powder, it is preferred that firing is performed so that the oxide fired body has 85% to 95% of the weight of the green body and/or has a volume that is greater than or equal to 90% of the volume of the green body.

Also, irrespective of whether or not the LDH powder is calcined, the relative density of the oxide fired body is preferably configured to be 20% to 40%, more preferably 20% to 35%, and still more preferably 20% to 30% with reference to an oxide conversion. A relative density with reference to an oxide conversion is a relative density that assumes that the respective metal elements that configure the LDH are converted into their respective oxides by firing, and is obtained with reference to a denominator that is calculated as a converted density of a mixture of each oxide.

The firing temperature for the green body may be configured as 400 degrees C. to 850 degrees C., and is preferably 700 degrees C. to 800 degrees C. The firing step preferably includes a step in which the above firing temperature is maintained for greater than or equal to 1 hour, and preferably 3 to 10 hours. Furthermore, the rate of temperature increase to reach a firing temperature is preferably less than or equal to 100 degrees C./h, more preferably 5 degrees C./h to 75 degrees C./h, and still more preferably 10 degrees C./h to 50 degrees C./h in order to prevent fracture of the green body that is caused by emission of moisture or carbon dioxide due to a sharp temperature increase. Therefore the total firing time from temperature increase to temperature decrease (less than or equal to 100 degrees C.) is preferably greater than or equal to 20 hours, more preferably 30 hours to 70 hours and still more preferably 35 hours to 65 hours.

When a pore forming agent is added to the green body in the preparation step for the green body as described above, pores are formed in an inner portion of the oxide fired body by firing and removal of the pore forming agent during the firing step.

4. Regeneration to LDH

Next, the oxide fired body is retained in or immediately above an aqueous solution that contains an n-valent anion (A^(n−)) as described above and is regenerated to LDH to thereby obtain an LDH solidified body that is moisture rich. That is to say, the LDH solidified body that is manufactured by this method unavoidably contains excess moisture.

It is noted that the anions that are contained in the aqueous solution may be the same anions as the anions that are contained in the LDH powder, or may be a different type of anion.

The retention of the oxide fired body in the aqueous solution or immediately above the aqueous solution is preferably performed by a method of hydrothermal synthesis in a sealed vessel. An example of a sealed vessel includes a sealed vessel manufactured from Teflon (Registered Trademark). The outer side of the sealed vessel preferably includes provision of a jacket of stainless steel or the like.

LDH conversion is preferably performed by retaining the oxide fired body at greater than or equal to 20 degrees C. and less than 200 degrees C., and in a state of contact of at least one surface of the oxide fired body with the aqueous solution. A more preferred temperature is 50 degrees C. to 180 degrees C. and a still more preferred temperature is 100 degrees C. to 150 degrees C. The oxide fired body is preferably retained for greater than or equal to 1 hour at this LDH conversion temperature, more preferably retained at greater than or equal to 2 hours, and still more preferably retained at greater than or equal to 5 hours. In this manner, sufficient regeneration to LDH is promoted while inhibiting residual heterogeneous phases. It is noted that although no problems arise in the event that the retention time is excessively long, suitable settings are appropriate when efficiency is taken into account.

Ion exchanged water can be used when using carbon dioxide (carbonate ions) in the air as a type of anion for the aqueous solution that contains n-valent anions that are used in regeneration to LDH. It is noted that when performing hydrothermal synthesis in a sealed vessel, the oxide fired body may be immersed in the aqueous solution, or may be treated in a state in which a jig is used and at least one surface makes contact with the aqueous solution. When treatment is performed in a state of contact of at least one surface with the aqueous solution, since the excess moisture amount is lower when compared with total immersion, subsequent treatment steps may be performed in less time. However, since crack formation tends to occur when the amount of aqueous solution is excessively low, it is preferred that an amount of moisture is used that is equivalent to or greater than the weight of the fired body.

It is noted that when pores are formed in an inner portion of the oxide fired body, even after the regeneration step, there will be residual pores in an inner portion of the LDH solidified body.

5. Dehydration Step

Next, an inorganic solid electrolyte 16 is obtained by removal of excess moisture from the LDH solidified body. The step of removal of excess moisture is preferably performed at less than or equal to 300 degrees C., and at greater than or equal to 25% of the estimated relative humidity at the maximum temperature of the removal step. When performing dehydration at a temperature that is higher than room temperature, it is preferred to re-enclose in the sealed vessel used in the LDH regeneration step in order to prevent rapid vaporization of the moisture from the LDH solidified body. The preferred temperature at that time is 50 degrees C. to 250 degrees C., with a temperature of 100 degrees C. to 200 degrees C. being more preferred. Furthermore, the more preferred relative humidity during dehydration is 25% to 70%, with 40% to 60% being still more preferred. Dehydration may be performed at room temperature and the relative humidity at that time may be configured to fall within a range of 40% to 70% of a normal indoor environment.

When the inorganic solid electrolyte 16 is exposed to an atmosphere containing carbon dioxide within the above concentration range means by means of the second method described above (method of providing through holes), the through holes are directly formed in the inorganic solid electrolyte 16 after removal of excess moisture. The through holes may be formed by using laser treatment or electrical discharge machining to open holes in the thickness direction of the inorganic solid electrolyte 16. The inner diameter of the through holes for example when using a laser treatment may be adjusted by varying the laser irradiation diameter or the irradiation pattern.

EXAMPLES

Although the examples of the present invention will be described below, the present invention is not thereby limited to the following examples.

Preparation Solid Alkaline Fuel Cell 10

(1) Preparation of Inorganic Solid Electrolyte 16

Firstly a starting material powder was prepared as a hydrotalcite powder (DHT-4H manufactured by Kyowa Chemical Industry Co., Ltd.) that is a commercially-available layered double hydroxide. The composition of the starting material powder was Mg²⁺ _(0.68)Al³⁺ _(0.32)(OH)₂CO₃ ²⁻ _(0.16).mH₂O. A disc-shaped die having a diameter of 20 mm was filled with the starting material powder and uniaxial press molding was performed at a molding pressure of 500 kgf/cm² to thereby obtain a green body exhibiting 53% relative density, 20 mm diameter and an approximate thickness of 0.8 mm. The measurement of the relative density was performed on a green body after storage for 24 hours at room temperature in a relative humidity of less than or equal to 20%.

Next, the resulting green body was fired in an alumina sheath. The rate of temperature increase during firing was less than or equal to 100 degrees C./h in order to prevent fracture of the green body caused by emission of moisture or carbon dioxide due to a sharp temperature increase. Then after reaching a maximum temperature of 750 degrees C., it was retained for 5 hours and allowed to cool. The total firing time from temperature increase to temperature decrease (less than or equal to 100 degrees C.) was 62 hours.

Next, the fired body was placed in a sealed vessel manufactured from Teflon (Registered Trademark) provided with an outer jacket of stainless steel and sealed together with ion exchange water in air. After performing hydrothermal synthesis on the fired body under regeneration conditions for a retention period of 5 hours at 100 degrees C., polishing was performed to a thickness of 0.3 mm and moisture on the fired body surface was wiped using filtration paper. In this manner, the inorganic solid electrolyte 16 was formed by natural dehydration (drying) indoors of the resulting fired body at 25 degrees C. and a relative humidity of 50%.

Next, in Examples 1 to 3 and Comparative Examples 2 and 3, through holes oriented in a thickness direction were formed in the inorganic solid electrolyte 16 by use of a laser. In that configuration, the carbon dioxide amount and the fuel amount that permeates the inorganic solid electrolyte 16 during the initial output measurement as described below were adjusted by controlling the laser output and the irradiation time to thereby adjust the inner diameter of the through holes.

2. Preparation of Cathode 12 and Anode 14

A platinum-supporting carbon having a Pt support amount of 50 wt % (TEC10E50E manufactured by Tanaka Kikinzoku Kogyo) (referred to below as “Pt/C”) and PVDF powder as a binder (referred to below as “PVDF binder”) were prepared. A cathode paste was prepared by mixing Pt/C, the PVDF binder and water into a paste so that the weight ratio of (Pt/C catalyst):(PVDF binder):(water) coincided with a ratio of 9 wt %:0.9 wt %:90 wt %.

In addition, a platinum/ruthenium-supporting carbon having a Pt—Ru support amount of 54 wt % (TEC61E54 manufactured by Tanaka Kikinzoku Kogyo) (referred to below as “Pt—Ru/C”) and PVDF binder were prepared. An anode paste was prepared by mixing Pt—Ru/C, the PVDF binder and water into a paste so that the weight ratio of (Pt—Ru/C catalyst):(PVDF binder):(water) coincided with a ratio of 9 wt %:0.9 wt %:90 wt %.

Next, the cathode paste was printed onto one surface of the inorganic solid electrolyte 16 and the anode paste was printed onto the other surface of the inorganic solid electrolyte 16. Then a conjugate of the cathode 12/inorganic solid electrolyte 16/anode 14 was formed by thermal treatment for 4 hours at a temperature of 180 degrees C. in N₂.

(3) Assembly of Solid Alkaline Fuel Cell 10

FIG. 2 is an exploded perspective view illustrating the solid alkaline fuel cell 10 that was prepared according to an Example.

Firstly the inorganic solid electrolyte 16 was fitted to a circular opening (diameter 20 mm) of an electrolyte fixing jig 218 and fixed by use of PTFE tape 220 that is provided with a circular opening 220 a having a diameter of 19 mm formed a central portion. It is noted that although the cathode 12 and the anode 14 were printed onto both surfaces of the inorganic solid electrolyte 16, FIG. 2 illustrates a configuration in which there is separation from the inorganic solid electrolyte 16.

Next, a gasket 222 (made of PTFE) formed with an opening 222 a, an air supply member 213 (made of carbon) for supply of humidified air and a current collecting plate 226 (made of gold plated copper) were stacked onto the cathode 12 side of the stacked body formed from the anode 14/inorganic solid electrolyte 16/cathode 12. The air supply member 213 is provided with a passage 213 a for allowing flow of humidified air and a slit (not shown) for supply of the humidified air to the cathode 12.

Next, a gasket 224 (made of PTFE) formed with an opening 224 a, a fuel supply member 215 (made of carbon) for supply of fuel and a current collecting plate 228 (made of gold plated copper) were stacked onto the anode 14 side of the stacked body formed from the anode 14/inorganic solid electrolyte 16/cathode 12. The fuel supply member 215 is provided with a passage 215 a for allowing flow of fuel and a slit 215 b for supply of the fuel to the anode.

The stacked body described above was finished by threadable attachment of screws 230 that were inserted into screw holes 226 a, 228 a formed in the four corners of the two current collecting plates 226, 228 to thereby complete the solid alkaline fuel cell 10.

Durability Testing of Solid Electrolyte 16

Firstly prior to assembly of the solid alkaline fuel cell 10, an infrared spectrometer (FT/IR-6200 type-A manufactured by JASCO Corporation) using a method of attenuated total reflection (ATR) acquired an infrared absorption spectrum of the cathode-side surface 16S of the solid electrolyte 16 and thereby measured an absorption wavelength of 1820 to 1650 cm⁻¹ indicating the intensity of carbon dioxide gas.

Next, the solid alkaline fuel cell 10 was heated to 120 degrees C.

Then, hydrogen was supplied to the fuel supply member 215 and was adjusted so that the fuel utilization ratio at the anode 14 was 50%. Next, a compressor was used to supply the air supply member 213 with a mixed gas of carbon dioxide and dry air at less than or equal to the dew point of 0 degrees C., and adjusted so that the air utilization ratio at the cathode 12 was 50%. At that time, the carbon dioxide mixture amount was adjusted to thereby vary the carbon dioxide concentration at the cathode-side surface 16S of the inorganic solid electrolyte 16 for each sample as shown in Table 1.

It is noted that the carbon dioxide centration at the cathode-side surface 16S was calculated by using gas chromatograph equipment to measure the oxidant that is totally recovered after passing through the cathode 12.

Then, after generating power for 720 hours at a rated load (0.3 A/cm²), the solid alkaline fuel cell 10 was disassembled to thereby expose the cathode-side surface 16S of the inorganic solid electrolyte 16, and an infrared spectrometer was used to acquire an infrared absorption spectrum of the cathode-side surface 16S and thereby measure an absorption wavelength of 1820 to 1650 cm⁻¹ indicating the intensity of carbon dioxide gas.

An intensity reduction rate (pre-power generation carbon dioxide gas intensity—post-power generation carbon dioxide gas intensity/pre-power generation carbon dioxide gas intensity) for carbon dioxide gas before and after power generation for 720 hours was calculated. Table 1 illustrates an evaluation when the intensity reduction rate for carbon dioxide gas was greater than or equal to 10% as X, and an evaluation when the intensity reduction rate for carbon dioxide gas was less than 10% as O.

Measurement of Initial Output of Solid Alkaline Fuel Cell 10

Firstly the solid alkaline fuel cell 10 was heated to 120 degrees C.

Next, a compressor was used to supply the air supply member 213 with dry air at less than or equal to the dew point of 0 degrees C., and was adjusted so that the air utilization ratio at the cathode 12 was 50%. Furthermore, gaseous methanol was supplied to the fuel supply member 215 and was adjusted so that the fuel utilization ratio at the anode 14 was 50%. The fuel pressure supplied to the anode 14 was adjusted to be greater than the air pressure supplied to the cathode 12 by use of a discharge pressure adjustment valve (not shown) that was mounted onto the respective discharge passages for the air supply member 213 and the fuel supply member 215.qq

Then, while generating power at a rated load (0.3 A/cm²), the initial output of the solid alkaline fuel cell 10 was measured. The initial output of each sample was standardized by taking the output of the solid alkaline fuel cell 10 according to Comparative Example 1 in which there is no provision of through holes in the inorganic solid electrolyte 16 as 100% and thereby an output reduction rate was calculated with reference to a standard using Comparative Example 1. Table 1 illustrates an evaluation when the output reduction rate was greater than or equal to 10% as X, and an evaluation when the output reduction rate was less than 10% as O.

TABLE 1 Carbon Dioxide Intensity Reduction Initial Concentration at Rate Of Carbon Output Cathode-side Surface Dioxide Gas Before/ of Solid Of Inorganic Solid After 720 Hours Alkaline Electrolyte (ppm) Power Generation Fuel Cell Example 1 600 ∘ ∘ Example 2 1000.0 ∘ ∘ Example 3 2000.0 ∘ ∘ Comparative N.D. (less than or x ∘ Example 1 equal to lower limit of detection) Comparative 500 x ∘ Example 2 Comparative 3000 ∘ x Example 3

As shown by Table 1, in Comparative Example 1 in which through holes were not formed in the inorganic solid electrolyte 16 and in Comparative Example 2 in which the cathode-side surface 16S was exposed to an atmosphere containing carbon dioxide of 500 ppm, the intensity reduction rate of carbon dioxide gas during durability testing of the solid electrolyte 16 was large. The reason for this result is considered to be the failure to improve the stability of CO3²⁻ that is coordinated between the LDH layers since the cathode-side surface 16S was not exposed to an atmosphere having a sufficiently high concentration of carbon dioxide. Furthermore, in Comparative Example 3 in which the cathode-side surface 16S was exposed to an atmosphere containing carbon dioxide of 3000 ppm, the initial output of the solid alkaline fuel cell 10 was low. The reason for this result is considered to be the adverse effect on the characteristics of the inorganic solid electrolyte 16 itself due to the fact that the ratio occupied by through holes relative to the inorganic solid electrolyte 16 was large.

On the other hand, in Examples 1 to 3 in which cathode-side surface 16S was exposed to an atmosphere containing carbon dioxide of greater than or equal to 600 ppm and less than or equal to 20000 ppm, the intensity reduction rate of carbon dioxide gas during durability testing of the solid electrolyte 16 was inhibited and the initial output of the solid alkaline fuel cell 10 was maintained. The reason for this result is considered to be the improvement in the stability of CO3²⁻ that is coordinated between the LDH layers as a result of exposing the cathode-side surface 16S to an atmosphere having a sufficiently high concentration of carbon dioxide and the fact that the characteristics of the inorganic solid electrolyte 16 itself were maintained. 

The invention claimed is:
 1. A method of power generation for a solid alkaline fuel cell, the solid alkaline fuel cell having a cathode, an anode, and an inorganic solid electrolyte disposed between the anode and the cathode and exhibiting hydroxide ion conductivity, the method comprising; exposing a cathode-side surface of the inorganic solid electrolyte to an atmosphere containing carbon dioxide of greater than or equal to 600 ppm and less than or equal to 20000 ppm. 